NDC 71335-1085 – Prazosin Hydrochloride

Prazosin Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1085

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210971
Marketed since
October 3, 2018
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Prazosin Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1085-130 CAPSULE in 1 BOTTLE (71335-1085-1)Feb 1, 2019
71335-1085-228 CAPSULE in 1 BOTTLE (71335-1085-2)Aug 19, 2026
71335-1085-360 CAPSULE in 1 BOTTLE (71335-1085-3)Nov 20, 2019
71335-1085-490 CAPSULE in 1 BOTTLE (71335-1085-4)Aug 19, 2026
71335-1085-518 CAPSULE in 1 BOTTLE (71335-1085-5)Aug 19, 2026

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